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Image Unavailable-BOSSBS-15262R-CY7

Anti-C7ORF29 Rabbit Polyclonal Antibody (Cy7)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.
Código de Artigo: BOSSBS-15262R-CY7
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15271R-HRP

Anti-C7ORF46 Rabbit Polyclonal Antibody (HRP)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf46 gene product has been provisionally designated C7orf46 pending further characterisation.
Código de Artigo: BOSSBS-15271R-HRP
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15274R-CY7

Anti-C7ORF57 Rabbit Polyclonal Antibody (Cy7)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf57 gene product has been provisionally designated C7orf57 pending further characterisation.
Código de Artigo: BOSSBS-15274R-CY7
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15273R-FITC

Anti-C7ORF53 Rabbit Polyclonal Antibody (FITC)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf53 gene product has been provisionally designated C7orf53 pending further characterisation.
Código de Artigo: BOSSBS-15273R-FITC
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15260R-CY7

Anti-C7ORF25 Rabbit Polyclonal Antibody (Cy7)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf25 gene product has been provisionally designated C7orf25 pending further characterisation.
Código de Artigo: BOSSBS-15260R-CY7
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-10471R

Anti-DYNC1I2 Rabbit Polyclonal Antibody

Descrição: The inner- and outer-arm dyneins, which bridge between the doublet microtubules in axonemes, are the force-generating proteins responsible for the sliding movement in axonemes. The intermediate and light chains, thought to form the base of the dynein arm, help mediate attachment and may also participate in regulating dynein activity. This gene encodes an intermediate chain dynein, belonging to the large family of motor proteins. Mutations in this gene result in abnormal ciliary ultrastructure and function associated with primary ciliary dyskinesia (PCD) and Kartagener syndrome. [provided by RefSeq, Jul 2008].
Código de Artigo: BOSSBS-10471R
UOM: 1 * 100 µl
Fornecedor: Bioss
Imagem do Produto-MFLX41507-13

Cadence Science Nickel-Plated Brass Luer Stopcocks

Descrição: Exceptional durability.
Código de Artigo: MFLX41507-13
UOM: 1 * 1 unid.
Fornecedor: Avantor Fluid Handling
Imagem do Produto-MIEL10973970

Accessories for Large Laboratory Glasswasher PLW 8616, PLW 8615 and PLW 8617

Descrição: Accessories for Glassware washing machines, A 603 Attachment for the expansion of the A 500 mobile unit to 2 levels. With spray arm, W×D×H: 640×790×565 mm
Código de Artigo: MIEL10973970
UOM: 1 * 1 unid.
Fornecedor: MIELE
Image Unavailable-BOSSBS-15261R-A555

Anti-C7ORF26 Rabbit Polyclonal Antibody (ALEXA FLUOR® 555)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf26 gene product has been provisionally designated C7orf26 pending further characterisation.
Código de Artigo: BOSSBS-15261R-A555
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15261R-A680

Anti-C7ORF26 Rabbit Polyclonal Antibody (ALEXA FLUOR® 680)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf26 gene product has been provisionally designated C7orf26 pending further characterisation.
Código de Artigo: BOSSBS-15261R-A680
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15279R-A647

Anti-C7ORF64 Rabbit Polyclonal Antibody (ALEXA FLUOR® 647)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf64 gene product has been provisionally designated C7orf64 pending further characterisation.
Código de Artigo: BOSSBS-15279R-A647
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15260R-A555

Anti-C7ORF25 Rabbit Polyclonal Antibody (ALEXA FLUOR® 555)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf25 gene product has been provisionally designated C7orf25 pending further characterisation.
Código de Artigo: BOSSBS-15260R-A555
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15269R-A555

Anti-C7ORF44 Rabbit Polyclonal Antibody (ALEXA FLUOR® 555)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf44 gene product has been provisionally designated C7orf44 pending further characterisation.
Código de Artigo: BOSSBS-15269R-A555
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15269R-A647

Anti-C7ORF44 Rabbit Polyclonal Antibody (ALEXA FLUOR® 647)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf44 gene product has been provisionally designated C7orf44 pending further characterisation.
Código de Artigo: BOSSBS-15269R-A647
UOM: 1 * 100 µl
Fornecedor: Bioss
Image Unavailable-BOSSBS-15257R-A488

Anti-C7ORF10 Rabbit Polyclonal Antibody (ALEXA FLUOR® 488)

Descrição: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf10 gene product has been provisionally designated C7orf10 pending further characterisation.
Código de Artigo: BOSSBS-15257R-A488
UOM: 1 * 100 µl
Fornecedor: Bioss
Imagem do Produto-139-0027

Particle counter transport cart

Descrição: This cart is specially designed for transporting particle sensing machines around the cleanroom environment. Stainless steel 304 with electropolished finish.
Código de Artigo: 139-0027
UOM: 1 * 1 unid.
Fornecedor: Palbam
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